潘尼斯电池
生物
干细胞
间充质干细胞
细胞生物学
Wnt信号通路
坏死性小肠结肠炎
细胞分化
肠道菌群
免疫学
类有机物
干细胞巢
微生物学
细胞
祖细胞
信号转导
小肠
内科学
遗传学
内分泌学
基因
医学
作者
Ji‐Eun Kim,Bo Li,Lijiang Fei,Rachael G. Horne,Dorothy Lee,Adrian Kwan Ho Loe,Hiromu Miyake,Eda Ayar,Maria Gurma,Dae‐Kyum Kim,Michael G. Surette,Dana J. Philpott,Philip M. Sherman,Guoji Guo,Agostino Pierro,Tae-Hee Kim
出处
期刊:Immunity
[Cell Press]
日期:2022-12-01
卷期号:55 (12): 2300-2317.e6
被引量:43
标识
DOI:10.1016/j.immuni.2022.11.003
摘要
Intestinal stem cell maturation and development coincide with gut microbiota exposure after birth. Here, we investigated how early life microbial exposure, and disruption of this process, impacts the intestinal stem cell niche and development. Single-cell transcriptional analysis revealed impaired stem cell differentiation into Paneth cells and macrophage specification upon antibiotic treatment in early life. Mouse genetic and organoid co-culture experiments demonstrated that a CD206+ subset of intestinal macrophages secreted Wnt ligands, which maintained the mesenchymal niche cells important for Paneth cell differentiation. Antibiotics and reduced numbers of Paneth cells are associated with the deadly infant disease, necrotizing enterocolitis (NEC). We showed that colonization with Lactobacillus or transfer of CD206+ macrophages promoted Paneth cell differentiation and reduced NEC severity. Together, our work defines the gut microbiota-mediated regulation of stem cell niches during early postnatal development.
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